40 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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G-CATH TISSUE ANCHOR DELIVERY CATHETER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169413726·BLADE 5102916 29MM WIDE VESSELBLADE 16CM
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964076879·The ENDO CARRY-ON Procedure Kit contains all of...
Plateau Spacer System
FDA UDI
Life Spine, Inc.·00190837026936·PLATEAU Interbody, Curved, Bulleted, 11mm 29mm ...
SURGI-VISION PROSTATE COIL
FDA 510(k)
FDA Class 2
·Radiology
FRONTIER ANTERIOR SCOLIOSIS SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
HLM TUBING SET
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·April 1, 2015
VKMO 70000 #QUADROX-I HMO 70000+VHK71
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTN·February 23, 2015
BO-HQV 70600#ADULT PACK
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTN·February 19, 2015
BO-HQV #70600ADULT PACK
FDA Adverse Event
Injury
·MAQUET CARDIOPULMONARY AG·Product code DTN·March 4, 2015
BO-HQV 70600#ADULT PACK
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DWE·March 27, 2015
BO-HQV 70600#ADULT PACK
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DWE·April 9, 2015
VKMO 11000
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 24, 2015
BO-HQV 70600 ADULT PACK
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTN·July 15, 2015
RESERVOIR VHK
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTN·July 28, 2015
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·January 25, 2012
VENOUS HARDSHELL CARDIOTOMY RESERVOIR
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTM·September 13, 2016
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Injury
·ANIMAS CORPORATION·Product code LZG·May 9, 2013
BREZE2
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE LLC·Product code NBW·September 19, 2014
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·May 4, 2011